RELB RELB proto-oncogene, NF-kB subunit

Information
Symbol
RELB
Type
protein-coding
Description
RELB proto-oncogene, NF-kB subunit
Entrez Gene ID
5971
Genome
hg19
Position
chr19:45,504,722-45,541,450
Genome
hg38
Position
chr19:45,001,464-45,038,192
MIM
604758 OMIM
HGNC
HGNC:9956 HGNC
Ensembl
ENSG00000104856 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 4
Benign 0 28
Likely benign 0 340
Uncertain significance 0 358
Ranking
ClinVar
0
0
54
672
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM I-REL
SYNONYM IMD53
SYNONYM IREL
SYNONYM REL-B
MIM 604758 OMIM
HGNC HGNC:9956 HGNC
Ensembl ENSG00000104856 Ensembl
AllianceGenome HGNC:9956
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000505236.2 hg38 chr19 45,001,461 45,037,790 36,330
ENST00000221452.13 hg38 chr19 45,001,464 45,038,192 36,729
ENST00000505236.2 hg19 chr19 45,504,719 45,541,048 36,330
ENST00000221452.13 hg19 chr19 45,504,722 45,541,450 36,729
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